5-Chloro-4-iodo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
98%
- Product Code: 124379
CAS:
1040682-76-5
| Molecular Weight: | 434.82 g./mol | Molecular Formula: | C₁₆H₂₄ClIN₂Si |
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| EC Number: | MDL Number: | MFCD09965903 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The triisopropylsilyl (TIPS) group serves as a protective moiety for the pyrrolopyridine nitrogen, enhancing stability and directing reactivity during synthetic transformations. Its applications are particularly relevant in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,593.00 |
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| 0.250 | 10-20 days | ฿2,700.00 |
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| 1.000 | 10-20 days | ฿7,281.00 |
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5-Chloro-4-iodo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
This compound is primarily utilized in organic synthesis as a versatile intermediate for the construction of complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both chloro and iodo substituents, allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. The triisopropylsilyl (TIPS) group serves as a protective moiety for the pyrrolopyridine nitrogen, enhancing stability and directing reactivity during synthetic transformations. Its applications are particularly relevant in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases.
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